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本文引用的文献

1
Dysregulation of CalDAG-GEFI and CalDAG-GEFII predicts the severity of motor side-effects induced by anti-parkinsonian therapy.钙依赖性鸟苷酸交换因子I(CalDAG-GEFI)和钙依赖性鸟苷酸交换因子II(CalDAG-GEFII)的失调预示着抗帕金森病治疗引起的运动副作用的严重程度。
Proc Natl Acad Sci U S A. 2009 Feb 24;106(8):2892-6. doi: 10.1073/pnas.0812822106. Epub 2009 Jan 26.
2
Intrabodies binding the proline-rich domains of mutant huntingtin increase its turnover and reduce neurotoxicity.与突变型亨廷顿蛋白富含脯氨酸结构域结合的胞内抗体可提高其周转率并降低神经毒性。
J Neurosci. 2008 Sep 3;28(36):9013-20. doi: 10.1523/JNEUROSCI.2747-08.2008.
3
Functional roles for the striatal-enriched transcription factor, Bcl11b, in the control of striatal gene expression and transcriptional dysregulation in Huntington's disease.纹状体富集转录因子Bcl11b在亨廷顿舞蹈病中对纹状体基因表达的调控及转录失调方面的功能作用。
Neurobiol Dis. 2008 Sep;31(3):298-308. doi: 10.1016/j.nbd.2008.05.005. Epub 2008 May 22.
4
Novel targets for Huntington's disease in an mTOR-independent autophagy pathway.亨廷顿舞蹈病在一条不依赖mTOR的自噬途径中的新型靶点。
Nat Chem Biol. 2008 May;4(5):295-305. doi: 10.1038/nchembio.79.
5
Mitogen- and stress-activated protein kinase-1 deficiency is involved in expanded-huntingtin-induced transcriptional dysregulation and striatal death.丝裂原和应激激活蛋白激酶-1缺乏参与了扩展型亨廷顿蛋白诱导的转录失调和纹状体死亡。
FASEB J. 2008 Apr;22(4):1083-93. doi: 10.1096/fj.07-9814. Epub 2007 Nov 20.
6
Inhibitors of metabolism rescue cell death in Huntington's disease models.代谢抑制剂可挽救亨廷顿舞蹈症模型中的细胞死亡。
Proc Natl Acad Sci U S A. 2007 Sep 4;104(36):14525-30. doi: 10.1073/pnas.0704482104. Epub 2007 Aug 28.
7
Essential role for Rap1 GTPase and its guanine exchange factor CalDAG-GEFI in LFA-1 but not VLA-4 integrin mediated human T-cell adhesion.Rap1 GTP酶及其鸟嘌呤交换因子CalDAG-GEFI在淋巴细胞功能相关抗原-1(LFA-1)而非极迟抗原-4(VLA-4)整合素介导的人T细胞粘附中起关键作用。
Blood. 2007 Nov 15;110(10):3682-90. doi: 10.1182/blood-2007-03-077628. Epub 2007 Aug 16.
8
Mutant huntingtin's effects on striatal gene expression in mice recapitulate changes observed in human Huntington's disease brain and do not differ with mutant huntingtin length or wild-type huntingtin dosage.突变型亨廷顿蛋白对小鼠纹状体基因表达的影响重现了在人类亨廷顿病大脑中观察到的变化,且与突变型亨廷顿蛋白的长度或野生型亨廷顿蛋白的剂量无关。
Hum Mol Genet. 2007 Aug 1;16(15):1845-61. doi: 10.1093/hmg/ddm133. Epub 2007 May 21.
9
Mice lacking the signaling molecule CalDAG-GEFI represent a model for leukocyte adhesion deficiency type III.缺乏信号分子CalDAG-GEFI的小鼠代表了III型白细胞黏附缺陷的一种模型。
J Clin Invest. 2007 Jun;117(6):1699-707. doi: 10.1172/JCI30575. Epub 2007 May 10.
10
Selective inhibitors of death in mutant huntingtin cells.突变亨廷顿蛋白细胞中死亡的选择性抑制剂。
Nat Chem Biol. 2007 Feb;3(2):99-100. doi: 10.1038/nchembio852. Epub 2006 Dec 31.

纹状体中 CalDAG-GEFI 的下调是亨廷顿病的一种神经保护变化。

CalDAG-GEFI down-regulation in the striatum as a neuroprotective change in Huntington's disease.

机构信息

McGovern Institute for Brain Research, MIT, 43 Vassar Street, Building 46-6133, Cambridge, MA, USA.

出版信息

Hum Mol Genet. 2010 May 1;19(9):1756-65. doi: 10.1093/hmg/ddq055. Epub 2010 Feb 10.

DOI:10.1093/hmg/ddq055
PMID:20147317
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2850620/
Abstract

Huntingtin protein (Htt) is ubiquitously expressed, yet Huntington's disease (HD), a fatal neurologic disorder produced by expansion of an Htt polyglutamine tract, is characterized by neurodegeneration that occurs primarily in the striatum and cerebral cortex. Such discrepancies between sites of expression and pathology occur in multiple neurodegenerative disorders associated with expanded polyglutamine tracts. One possible reason is that disease-modifying factors are tissue-specific. Here, we show that the striatum-enriched protein, CalDAG-GEFI, is severely down-regulated in the striatum of mouse HD models and is down-regulated in HD individuals. In the R6/2 transgenic mouse model of HD, striatal neurons with the largest aggregates of mutant Htt have the lowest levels of CalDAG-GEFI. In a brain-slice explant model of HD, knock-down of CalDAG-GEFI expression rescues striatal neurons from pathology induced by transfection of polyglutamine-expanded Htt exon 1. These findings suggest that the striking down-regulation of CalDAG-GEFI in HD could be a protective mechanism that mitigates Htt-induced degeneration.

摘要

亨廷顿蛋白(Htt)广泛表达,但亨廷顿病(HD)是一种由 Htt 多聚谷氨酰胺片段扩展引起的致命神经退行性疾病,其特征是主要发生在纹状体和大脑皮层的神经退行性变。在与多聚谷氨酰胺片段扩展相关的多种神经退行性疾病中,存在着表达部位与病理学之间的这种差异。一个可能的原因是疾病修饰因子是组织特异性的。在这里,我们表明富含纹状体的蛋白 CalDAG-GEFI 在小鼠 HD 模型的纹状体中严重下调,并且在 HD 个体中下调。在 R6/2 转基因 HD 小鼠模型中,具有最大突变 Htt 聚集体的纹状体神经元中 CalDAG-GEFI 的水平最低。在 HD 的脑切片外植体模型中,CalDAG-GEFI 表达的敲低可挽救由转染多聚谷氨酰胺扩展的 Htt 外显子 1 引起的纹状体神经元的病理。这些发现表明,HD 中 CalDAG-GEFI 的显著下调可能是一种保护机制,可以减轻 Htt 诱导的变性。